CA2642983A1 - Multifunctional star-shaped prepolymers, their preparation and use - Google Patents
Multifunctional star-shaped prepolymers, their preparation and use Download PDFInfo
- Publication number
- CA2642983A1 CA2642983A1 CA002642983A CA2642983A CA2642983A1 CA 2642983 A1 CA2642983 A1 CA 2642983A1 CA 002642983 A CA002642983 A CA 002642983A CA 2642983 A CA2642983 A CA 2642983A CA 2642983 A1 CA2642983 A1 CA 2642983A1
- Authority
- CA
- Canada
- Prior art keywords
- star
- shaped
- prepolymer
- prepolymers
- groups
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
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- 238000009827 uniform distribution Methods 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Chemical group 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/91—Graft copolymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
- C08G18/485—Polyethers containing oxyethylene units and other oxyalkylene units containing mixed oxyethylene-oxypropylene or oxyethylene-higher oxyalkylene end groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5036—Polyethers having heteroatoms other than oxygen having nitrogen containing -N-C=O groups
- C08G18/5045—Polyethers having heteroatoms other than oxygen having nitrogen containing -N-C=O groups containing urethane groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5096—Polyethers having heteroatoms other than oxygen containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/71—Monoisocyanates or monoisothiocyanates
- C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
- C09D171/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09D201/10—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/544—Dendrimers, Hyperbranched polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/94—Involves covalent bonding to the substrate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2210/00—Compositions for preparing hydrogels
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Public Health (AREA)
- Materials Engineering (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Paints Or Removers (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyethers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006009004.7 | 2006-02-23 | ||
| DE102006009004A DE102006009004A1 (de) | 2006-02-23 | 2006-02-23 | Multifunktionelle sternförmige Präpolymere, deren Herstellung und Verwendung |
| PCT/EP2007/001056 WO2007096056A1 (de) | 2006-02-23 | 2007-02-08 | Multifunktionelle sternförmige präpolymere, deren herstellung und verwendung |
Publications (1)
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| CA2642983A1 true CA2642983A1 (en) | 2007-08-30 |
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| CA002642983A Abandoned CA2642983A1 (en) | 2006-02-23 | 2007-02-08 | Multifunctional star-shaped prepolymers, their preparation and use |
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| EP (1) | EP1987080A1 (https=) |
| JP (1) | JP2009527603A (https=) |
| CN (1) | CN101389690A (https=) |
| BR (1) | BRPI0708083A2 (https=) |
| CA (1) | CA2642983A1 (https=) |
| DE (1) | DE102006009004A1 (https=) |
| WO (1) | WO2007096056A1 (https=) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
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| SG170829A1 (en) * | 2006-04-04 | 2011-05-30 | Basf Se | Bleach systems enveloped with polymeric layers |
| DE102007020404A1 (de) * | 2006-09-18 | 2008-10-30 | Nano-X Gmbh | Verfahren zur Herstellung eines Beschichtungsmaterials |
| DE102006044310A1 (de) * | 2006-09-18 | 2008-03-27 | Nano-X Gmbh | Silanbeschichtungsmaterial und Verfahren zur Herstellung eines Silanbeschichtungsmaterials |
| DE102007038455A1 (de) * | 2007-08-14 | 2009-02-19 | Henkel Ag & Co. Kgaa | Polycarbonat-, Polyurethan- und/oder Polyharnstoff-Polyorganosiloxan-Verbindungen als die Primärwaschkraft verbessernde Wirkstoffe |
| DE102007039665A1 (de) * | 2007-08-22 | 2009-02-26 | Sustech Gmbh & Co. Kg | Silylfunktionelle lineare Präpolymere, deren Herstellung und Verwendung |
| DE102007039648A1 (de) * | 2007-08-22 | 2009-02-26 | Sustech Gmbh & Co. Kg | Mischungen, multifunktioneller sternförmiger Präpolymere, deren Herstellung und Verwendung sowie Beschichtungen daraus |
| DE102007055703A1 (de) * | 2007-12-04 | 2009-06-10 | Wacker Chemie Ag | Siliconhaltiger Polyurethanschaum |
| JP2011514255A (ja) * | 2008-03-18 | 2011-05-06 | ナノ−エックス ゲーエムベーハー | 高耐摩耗性の乗り物用塗料の製造方法、乗り物用塗料、およびその使用 |
| DE102008001384A1 (de) * | 2008-04-25 | 2009-10-29 | Wacker Chemie Ag | Siliconhaltiger Polyisocyanuratschaum |
| DE102008064197A1 (de) | 2008-12-22 | 2010-07-01 | Henkel Ag & Co. Kgaa | Adsorptionsmittel zur Abtrennung gefärbter Verbindungen aus wässrigen Zubereitungen |
| DE102008063070A1 (de) * | 2008-12-23 | 2010-07-01 | Henkel Ag & Co. Kgaa | Verwendung sternförmiger Polymere mit peripheren negativ geladenen Gruppen und/oder peripheren Silyl-Gruppen zur Ausrüstung von Oberflächen |
| DE102009028209A1 (de) * | 2009-08-04 | 2011-02-10 | Henkel Ag & Co. Kgaa | Haarbehandlungsmittel mit Polyether-modifizierten organischen Verbindungen und haarfestigenden Polymeren |
| DE102009029060A1 (de) | 2009-09-01 | 2011-03-03 | Henkel Ag & Co. Kgaa | Mittel zur Behandlung harter Oberflächen |
| WO2011075185A1 (en) | 2009-12-18 | 2011-06-23 | Oligasis | Targeted drug phosphorylcholine polymer conjugates |
| BR112012026118B1 (pt) * | 2010-04-15 | 2021-01-05 | Oligasis | polímeros de alto peso molecular contendo zwitterion |
| US9522980B2 (en) | 2010-05-06 | 2016-12-20 | Johnson & Johnson Vision Care, Inc. | Non-reactive, hydrophilic polymers having terminal siloxanes and methods for making and using the same |
| DE102010032780A1 (de) | 2010-07-26 | 2012-01-26 | Helfried Haufe | Hydrophile Schicht und Beschichtungszusammensetzung zur Herstellung der Schicht sowie Verfahren zur Herstellung der Beschichtungszusammensetzung |
| US20130203813A1 (en) | 2011-05-04 | 2013-08-08 | Johnson & Johnson Vision Care, Inc. | Medical devices having homogeneous charge density and methods for making same |
| US9170349B2 (en) | 2011-05-04 | 2015-10-27 | Johnson & Johnson Vision Care, Inc. | Medical devices having homogeneous charge density and methods for making same |
| EP2726870B1 (en) | 2011-06-29 | 2018-10-03 | Academia Sinica | The capture, purification and release of biological substance using a surface coating |
| FR2982158B1 (fr) * | 2011-11-09 | 2014-06-20 | Oreal | Composition cosmetique ou dermatologique comprenant un alpha-alcoxysilane obtenu a partir d'un epoxyde |
| US9297929B2 (en) | 2012-05-25 | 2016-03-29 | Johnson & Johnson Vision Care, Inc. | Contact lenses comprising water soluble N-(2 hydroxyalkyl) (meth)acrylamide polymers or copolymers |
| US10073192B2 (en) | 2012-05-25 | 2018-09-11 | Johnson & Johnson Vision Care, Inc. | Polymers and nanogel materials and methods for making and using the same |
| US9244196B2 (en) | 2012-05-25 | 2016-01-26 | Johnson & Johnson Vision Care, Inc. | Polymers and nanogel materials and methods for making and using the same |
| WO2014126599A1 (en) | 2013-02-15 | 2014-08-21 | Momentive Performance Materials Inc. | Antifouling system comprising silicone hydrogel |
| WO2015035342A2 (en) | 2013-09-08 | 2015-03-12 | Oligasis Llc | Factor viii zwitterionic polymer conjugates |
| TW201623605A (zh) | 2014-04-01 | 2016-07-01 | 中央研究院 | 用於癌症診斷及預後之方法及系統 |
| US9840553B2 (en) | 2014-06-28 | 2017-12-12 | Kodiak Sciences Inc. | Dual PDGF/VEGF antagonists |
| US9782727B2 (en) | 2014-07-14 | 2017-10-10 | International Business Machines Corporation | Filtration membranes with functionalized star polymers |
| US10112198B2 (en) | 2014-08-26 | 2018-10-30 | Academia Sinica | Collector architecture layout design |
| KR20210013299A (ko) | 2014-10-17 | 2021-02-03 | 코디악 사이언시스 인코포레이티드 | 부티릴콜린에스테라제 양성이온성 중합체 컨쥬게이트 |
| CN104722242B (zh) * | 2015-01-27 | 2016-09-28 | 南方科技大学 | 星形/多臂嵌段共聚物在制备含有纳米粒子的混合物中的用途 |
| US12534576B2 (en) | 2015-01-28 | 2026-01-27 | Dow Silicones Corporation | Elastomeric compositions and their applications |
| US10563015B2 (en) | 2015-01-28 | 2020-02-18 | Dow Silicones Corporation | Elastomeric compositions and their applications |
| US10005042B2 (en) | 2015-02-16 | 2018-06-26 | International Business Machines Corporation | Thin film composite forward osmosis membranes with performance enhancing layers |
| US9931598B2 (en) | 2015-02-16 | 2018-04-03 | International Business Machines Corporation | Anti-fouling coatings with star polymers for filtration membranes |
| FR3044222B1 (fr) * | 2015-11-30 | 2020-01-03 | L'oreal | Procede de traitement cosmetique des matieres keratiniques |
| KR20250057128A (ko) | 2015-12-30 | 2025-04-28 | 코디악 사이언시스 인코포레이티드 | 항체 및 이의 접합체 |
| US10107726B2 (en) | 2016-03-16 | 2018-10-23 | Cellmax, Ltd. | Collection of suspended cells using a transferable membrane |
| GB201613399D0 (en) | 2016-08-03 | 2016-09-14 | Dow Corning | Cosmetic composition comprising silicone materials |
| GB201613397D0 (en) | 2016-08-03 | 2016-09-14 | Dow Corning | Cosmetic composition comprising silicone materials |
| GB201707439D0 (en) | 2017-05-09 | 2017-06-21 | Dow Corning | Lamination Process |
| GB201707437D0 (en) | 2017-05-09 | 2017-06-21 | Dow Corning | Lamination adhesive compositions and their applications |
| PL3649164T3 (pl) | 2017-07-07 | 2022-01-31 | Repsol, S.A. | Modyfikowane poliole polimerowe |
| CA3084599C (en) * | 2017-12-14 | 2021-12-21 | Akzo Nobel Coatings International B.V. | Substrate coated with a multi-layer coating system and a process for controlling aquatic biofouling on man-made objects using such multi-layer coating system |
| EP3758737A4 (en) | 2018-03-02 | 2022-10-12 | Kodiak Sciences Inc. | IL-6 ANTIBODIES AND FUSION CONSTRUCTS AND CONJUGATES THEREOF |
| WO2020202071A1 (en) * | 2019-04-05 | 2020-10-08 | Sabic Global Technologies B.V. | Semi-crystalline silyl ether based vitrimers, methods of making and uses thereof |
| CA3157509A1 (en) | 2019-10-10 | 2021-04-15 | Kodiak Sciences Inc. | Methods of treating an eye disorder |
| EP3838962A1 (en) * | 2019-12-20 | 2021-06-23 | Repsol, S.A. | Stable modified polymer polyol dispersions |
| RS65063B1 (sr) | 2019-12-20 | 2024-02-29 | Repsol Sa | Disperzije stabilnih modifikovanih polimer poliola |
| DE102020112185A1 (de) | 2020-05-06 | 2021-11-11 | Volkswagen Aktiengesellschaft | Wärmeübertrager für ein Fahrzeug |
| IL301609A (en) * | 2020-10-01 | 2023-05-01 | Standard Millox Pharmaceuticals Oy | Hydrogel material |
| EP4306570A4 (en) * | 2021-03-12 | 2025-03-05 | Agc Inc. | HARDENABLE COMPOSITION AND HARDENED PRODUCT |
| WO2023210470A1 (ja) * | 2022-04-26 | 2023-11-02 | Ａｇｃ株式会社 | 化合物、組成物、表面処理剤、物品の製造方法、及び物品 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3354022A (en) * | 1964-03-31 | 1967-11-21 | Du Pont | Water-repellant surface |
| US3985830B1 (en) * | 1974-07-15 | 1998-03-03 | Univ Akron | Star polymers and process for the preparation thereof |
| US4480072A (en) * | 1982-03-10 | 1984-10-30 | Union Carbide Corporation | Use of ethyl silicate as a crosslinker for hydroxylated polymers |
| DE69115535T2 (de) * | 1990-03-23 | 1996-06-13 | Ici Plc | Polymere |
| SE9200564L (sv) * | 1992-02-26 | 1993-03-15 | Perstorp Ab | Dendritisk makromolekyl av polyestertyp, foerfarande foer framstaellning daerav samt anvaendning daerav |
| JPH0995609A (ja) * | 1995-09-29 | 1997-04-08 | Asahi Glass Co Ltd | 室温硬化性組成物およびその製造方法 |
| US5830986A (en) * | 1996-10-28 | 1998-11-03 | Massachusetts Institute Of Technology | Methods for the synthesis of functionalizable poly(ethylene oxide) star macromolecules |
| US5739218A (en) * | 1997-06-02 | 1998-04-14 | Dow Corning Corporation | Radially layered copoly (amidoamine-organosilicon) dendrimers |
| US5902863A (en) * | 1997-07-21 | 1999-05-11 | Dow Corning Corporation | Dendrimer-based networks containing lyophilic organosilicon and hydrophilic polyamidoamine nanoscopic domains |
| AR019107A1 (es) * | 1998-04-27 | 2001-12-26 | Dow Global Technologies Inc | Polioles de alto peso molecular, proceso para su preparacion y uso de los mismos. |
| JP2002513047A (ja) * | 1998-04-27 | 2002-05-08 | ザ ユニバーシティ オブ アクロン | 超分子構造体及びその製法 |
| US6001945A (en) * | 1998-07-15 | 1999-12-14 | Dow Corning Corporation | Hyperbranched polymers containing silicon atoms |
| JP2000109676A (ja) * | 1998-10-08 | 2000-04-18 | Asahi Glass Co Ltd | 硬化性組成物 |
| JP2000109678A (ja) * | 1998-10-08 | 2000-04-18 | Asahi Glass Co Ltd | 改良された室温硬化性組成物 |
| DE19924674C2 (de) * | 1999-05-29 | 2001-06-28 | Basf Coatings Ag | Thermisch und mit aktinischer Strahlung härtbarer Beschichtungsstoff und seine Verwendung |
| BR0107942A (pt) * | 2000-01-28 | 2004-01-06 | Infimed Therapeutics Inc | Polìmeros de proteìna de liberação lenta |
| US6350384B1 (en) * | 2000-08-14 | 2002-02-26 | Dow Corning Corporation | Silicon containing multi-arm star polymers |
| US20020027921A1 (en) * | 2000-08-15 | 2002-03-07 | Brinskele Edward A. | Apparatus and methods for providing hosted services over an asynchronous transfer mode connection |
| DE10048615A1 (de) * | 2000-09-30 | 2002-04-11 | Degussa | Nichtwäßriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
| GB0025211D0 (en) * | 2000-10-14 | 2000-11-29 | Avecia Bv | Hyperbranched compositions |
| US6534600B2 (en) * | 2001-03-26 | 2003-03-18 | Michigan Molecular Institute | Hyperbranched polyureas, polyurethanes, polyamidoamines, polyamides and polyesters |
| JP3824071B2 (ja) * | 2001-12-25 | 2006-09-20 | 信越化学工業株式会社 | 室温硬化性オルガノポリシロキサン組成物 |
| EP1469893A1 (de) * | 2002-02-01 | 2004-10-27 | Sustech GmbH & Co. KG | Sternformige prapolymere fur die herstellung ultradunner hydrogel-bildender beschichtungen |
| DE10204523A1 (de) * | 2002-02-05 | 2003-08-07 | Bayer Ag | Alkoxysilan- und OH-Endgruppen aufweisende Polyurethanprepolymere mit erniedrigter Funktionalität, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung |
| US6953787B2 (en) * | 2002-04-12 | 2005-10-11 | Arena Pharmaceuticals, Inc. | 5HT2C receptor modulators |
| KR20040040782A (ko) * | 2002-11-08 | 2004-05-13 | 선바이오(주) | 신규한 헥사-암 폴리에틸렌글리콜과 유도체 및 그의합성방법 |
| KR100578737B1 (ko) * | 2003-06-25 | 2006-05-12 | 학교법인 포항공과대학교 | 반응성 방사구조 고분자 및 이를 이용한 저유전성 고분자복합체 박막 |
| DE10329723B3 (de) * | 2003-07-02 | 2004-12-02 | Clariant Gmbh | Alkoxylierte Dendrimere und ihre Verwendung als biologisch abbaubare Emulsionsspalter |
| DE102004031938A1 (de) * | 2003-07-07 | 2005-01-27 | Sustech Gmbh & Co. Kg | Sternförmige Präpolymere für die bakteriostatische Ausrüstung von Oberflächen |
| EP1496079B1 (de) * | 2003-07-10 | 2005-07-06 | Wacker-Chemie GmbH | Vernetzbare Siloxan-Harnstoff-Copolymere |
| KR100554157B1 (ko) * | 2003-08-21 | 2006-02-22 | 학교법인 포항공과대학교 | 저유전 특성의 유기 실리케이트 고분자 복합체 |
| JP5096308B2 (ja) * | 2005-03-10 | 2012-12-12 | マサチューセッツ インスティテュート オブ テクノロジー | 超疎水性ファイバー、並びにその作成及び使用方法 |
| TWI379849B (en) * | 2005-09-20 | 2012-12-21 | Eternal Chemical Co Ltd | Radiation-curable alkoxy silanized hyperbranched polyester acrylates and preparation thereof |
-
2006
- 2006-02-23 DE DE102006009004A patent/DE102006009004A1/de not_active Withdrawn
-
2007
- 2007-02-08 BR BRPI0708083-2A patent/BRPI0708083A2/pt not_active Application Discontinuation
- 2007-02-08 CA CA002642983A patent/CA2642983A1/en not_active Abandoned
- 2007-02-08 CN CNA200780006531XA patent/CN101389690A/zh active Pending
- 2007-02-08 JP JP2008555661A patent/JP2009527603A/ja active Pending
- 2007-02-08 EP EP07722790A patent/EP1987080A1/de not_active Withdrawn
- 2007-02-08 WO PCT/EP2007/001056 patent/WO2007096056A1/de not_active Ceased
-
2008
- 2008-08-20 US US12/194,834 patent/US20090029043A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20090029043A1 (en) | 2009-01-29 |
| DE102006009004A1 (de) | 2007-09-06 |
| WO2007096056A1 (de) | 2007-08-30 |
| JP2009527603A (ja) | 2009-07-30 |
| EP1987080A1 (de) | 2008-11-05 |
| CN101389690A (zh) | 2009-03-18 |
| BRPI0708083A2 (pt) | 2011-05-17 |
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